Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: NTF3[original query] |
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Novel polymorphisms in the promoter region of the neurotrophin-3 gene and their associations with schizophrenia. American journal of medical genetics 2002 Apr 114 (3): 304-9. Hattori Mineko, Kunugi Hiroshi, Akahane Akihisa, Tanaka Hiroshi, Ishida Sugiko, Hirose Tetsuya, Morita Ryoji, Yamakawa Kazuhiro, Nanko Shinichi |
Analysis of enhancer activity of a dinucleotide repeat polymorphism in the neurotrophin-3 gene and its association with bipolar disorder. Neuropsychobiology 2004 50 (3): 206-10. Tadokoro K, Hashimoto R, Tatsumi M, Kamijima K, Kunugi |
Neurotrophic factor-related gene polymorphisms and adult attention deficit hyperactivity disorder (ADHD) score in a high-risk male population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Dec 147B (8): 1476-80. Conner Alex C, Kissling Christian, Hodges Edward, Hünnerkopf Regina, Clement R Marc, Dudley Edward, Freitag Christine M, Rösler Michael, Retz Wolfgang, Thome Johann |
A novel point variant in NTRK3, R645C, suggests a role of this gene in the pathogenesis of Hirschsprung disease. Annals of human genetics 2009 Jan 73 (1): 19-25. Fernández R M, Sánchez-Mejías A, Mena M D, Ruiz-Ferrer M, López-Alonso M, Antiñolo G, Borrego |
Association study of 10 genes encoding neurotrophic factors and their receptors in adult and child attention-deficit/hyperactivity disorder. Biological psychiatry 2008 May 63 (10): 935-45. Ribasés Marta, Hervás Amaia, Ramos-Quiroga Josep Antoni, Bosch Rosa, Bielsa Anna, Gastaminza Xavier, Fernández-Anguiano Mònica, Nogueira Mariana, Gómez-Barros Núria, Valero Sergi, Gratacòs Mònica, Estivill Xavier, Casas Miquel, Cormand Bru, Bayés Mòni |
Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders. Human molecular genetics 2008 May 17 (9): 1234-44. Mercader Josep Maria, Saus Ester, Agüera Zaida, Bayés Mònica, Boni Claudette, Carreras Anna, Cellini Elena, de Cid Rafael, Dierssen Mara, Escaramís Geòrgia, Fernández-Aranda Fernando, Forcano Laura, Gallego Xavier, González Juan Ramón, Gorwood Philip, Hebebrand Johannes, Hinney Anke, Nacmias Benedetta, Puig Anna, Ribasés Marta, Ricca Valdo, Romo Lucia, Sorbi Sandro, Versini Audrey, Gratacòs Mònica, Estivill Xavi |
Neurotrophin-3 gene, intelligence, and selective attention deficit in a Korean sample with attention-deficit/hyperactivity disorder. Progress in neuro-psychopharmacology & biological psychiatry 2010 Aug 34 (6): 1065-9. Cho Soo-Churl, Kim Hyo-Won, Kim Boong-Nyun, Kim Jae-Won, Shin Min-Sup, Cho Dae-Yeon, Chung Seockhoon, Jung Sun-Woo, Yoo Hee Jeong, Chung In-Won, Chung Un-Sun, Son Jung-W |
A promoter polymorphism of neurotrophin 3 gene is associated with curve severity and bracing effectiveness in adolescent idiopathic scoliosis. Spine 2012 Jan 37 (2): 127-33. Qiu Yong, Mao Sai-hu, Qian Bang-ping, Jiang Jun, Qiu Xu-sheng, Zhao Qinghua, Liu Zh |
Neurotrophin serum concentrations and polymorphisms of neurotrophins and their receptors in children with asthma. Respiratory medicine 2013 Jan 107 (1): 30-6. Szczepankiewicz Aleksandra, Rachel Marta, Sobkowiak Paulina, Kycler Zdzis?awa, Wojsyk-Banaszak Irena, Schöneich Natalia, Szczawi?ska-Pop?onyk Aleksandra, Br?borowicz An |
The relationship between the presence of ADHD and certain candidate gene polymorphisms in a Turkish sample. Gene 2013 Oct 528 (2): 320-7. Pazvanto?lu Ozan, Güne? Sezgin, Karabekiro?lu Koray, Ye?in Zeynep, Erenku? Zehra, Akba? Seher, Sar?soy Gökhan, Korkmaz I??l Zabun, Böke Omer, Ba?c? Hasan, Sahin Ahmet Rif |
Neurotrophin 3 genotype and emotional adverse effects of osmotic-release oral system methylphenidate (OROS-MPH) in children with attention-deficit/hyperactivity disorder. Journal of psychopharmacology (Oxford, England) 2014 Mar 28 (3): 220-6. Park Subin, Kim Bung-Nyun, Kim Jae-Won, Shin Min-Sup, Cho Soo-Churl, Kim Ji-Hoon, Son Jung-Woo, Shin Yun-Mi, Chung Un-Sun, Han Doug-Hy |
Genetics of long-term treatment outcome in bipolar disorder.
Progress in neuro-psychopharmacology & biological psychiatry 2016 Feb 65 17-24. Fabbri Chiara, Serretti Alessand |
A missense variant rs2585405 in clock gene PER1 is associated with the increased risk of noise-induced hearing loss in a Chinese occupational population. BMC medical genomics 2021 Sep 14 (1): 221. Chen Hao, Ding Xuexue, Ding Enmin, Chen Mengyao, Wang Huimin, Yang Guangzhi, Zhu Bao |
Predictive value of single-nucleotide polymorphisms in curve progression of adolescent idiopathic scoliosis. European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society 2022 4 31 (9): 2311-2325. Wang Wengang, Chen Tailong, Liu Yibin, Wang Songsong, Yang Ningning, Luo Mi |
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- Page last updated:Apr 22, 2024
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